| P594 | Ensembl gene ID | ENSG00000161671 |
| P704 | Ensembl transcript ID | ENST00000334976 |
| ENST00000376918 | ||
| ENST00000594508 | ||
| ENST00000597426 | ||
| ENST00000597799 | ||
| ENST00000598585 | ||
| ENST00000599293 | ||
| ENST00000601780 | ||
| P351 | Entrez Gene ID | 284361 |
| P2888 | exact match | http://identifiers.org/ncbigene/284361 |
| P2671 | Google Knowledge Graph ID | /g/11gbldv8c_ |
| P353 | HGNC gene symbol | EMC10 |
| P354 | HGNC ID | 27609 |
| P593 | HomoloGene ID | 18036 |
| P492 | OMIM ID | 614545 |
| 614545 | ||
| P639 | RefSeq RNA ID | NM_175063 |
| NM_206538 | ||
| P2892 | UMLS CUI | C2240327 |
| P1057 | chromosome | human chromosome 19 | Q510786 |
| P4196 | cytogenetic location | 19q13.33 | |
| P688 | encodes | ER membrane protein complex subunit 10 | Q21132216 |
| ER membrane protein complex subunit 10 | Q21150975 | ||
| P5572 | expressed in | anterior pituitary | Q356002 |
| right coronary artery | Q429285 | ||
| ascending aorta | Q2349469 | ||
| right testis | Q66502829 | ||
| right lobe of thyroid gland | Q66508047 | ||
| left lobe of thyroid gland | Q66508049 | ||
| C1 segment | Q66569011 | ||
| stromal cell of endometrium | Q66592424 | ||
| Descending thoracic aorta | Q66592966 | ||
| right adrenal gland | Q66715642 | ||
| P703 | found in taxon | Homo sapiens | Q15978631 |
| P645 | genomic end | 50490871 | |
| 50986608 | |||
| P644 | genomic start | 50476400 | |
| 50979657 | |||
| P684 | ortholog | Emc10 | Q18263879 |
| Emc10 | Q24411342 | ||
| EMC10 | Q29733904 | ||
| emc10 | Q29771982 | ||
| P2548 | strand orientation | forward strand | Q22809680 |
| Q27594379 | hsa-miR-185-5p |
| Q27593295 | hsa-miR-2276-5p |
| Q27594011 | hsa-miR-3190-5p |
| Q27595256 | hsa-miR-361-3p |
| Q27593480 | hsa-miR-377-3p |
| Q27594970 | hsa-miR-3926 |
| Q27592743 | hsa-miR-4684-5p |
| Q27593229 | hsa-miR-548c-3p |
| Q27594137 | hsa-miR-548s |
| Q27594004 | hsa-miR-642a-5p |
| Q27593769 | hsa-miR-6884-3p |
| Q27594946 | hsa-miR-6892-3p |
| Q27592811 | hsa-miR-760 |
| Q27594154 | hsa-miR-8485 |
| Q67131076 | 22q11.2 copy number variation syndrome | has part(s) | P527 |
| Tatar language (tt / Q25285) | EMC10 | wikipedia |
| EMC10 | wikipedia |
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